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DESIGN AND SYNTHESIS OF A NEW CHELATE FOR THE URANYL ION Yael Alboa, Eric Maimona,b*, Israel Zilbermanna,b, Magal Saphiera,b, and Dan Meyersteina,c* Chemistry Department, Ben Gurion University of the Negev, Beer Sheva, Israel e-mail: [email protected] Nuclear Research Centre Negev, Beer Sheva, Israel Biological Chemistry Department, College of Judea and Samaria, Ariel, Israel The hard acid, large uranyl cation is expected to form stable complexes with diamino tetradentate dianionic open chain ligands. As the two axial position of the dioxo cation are occupied it was decided to design a flexible ligand, which will be able to adjust itself to the coordination demands of the central metal ion in the equatorial plane. Herein we report of a new chelate agent for the uranyl cation – N,N’- di(2-hydroxy-4,6-di tertbutyl benzyl) imidazolidine. This tetradentate ligand is expected to coordinate uranyl ion, leaving a free fifth equatorial coordination site for complexation with an additional monodentate ligand. The ligand has been characterized by NMR and elemental analysis. This ligand reacts instantaneously with uranyl ion to give a red solution with two characteristic absorption bands in the visible region. Thus it was decided to examine the possibility of development of a new quantitative spectrophotometric method for the determination of the uranyl ion concentration in aqueous solutions. Preliminary experiments give encouraging results regarding the possibility that this ligand can be used as reagent for the determination of uranyl ions’ concentrations in aqueous solutions, in the 5·10-5 M – 1.5·10-4 M concentration range, or as a colorimetric sensor for determining the presence of uranyl ions in solution.